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Replies to "I have had facial pain for a long time. I have been wearing a hard plastic..."
Welcome @karencecilia and @chefcole. Being newly diagnosed with Eagle syndrome can be scary. But you're not alone. Here you'll meet many members, like @hoping @hdeshazer @rondam @bitoberry @mindyf @vbammer @pam71 @brooklyngirl @meliss @de9g @elimpert96 @jchristophersen @alcorreia0123 @empy @abby4paige @theeaglehasland @keetee @jenlink @fayzaibrahim @rosie68 @christina61 @stacybf @ladylove1962 @kariheppner @marjana @rosie68 and more who have shared their experiences in this related discussion:
- Eagle Syndrome https://connect.mayoclinic.org/discussion/eagles-syndrome/
What, if any, treatment or management approaches have been suggested for you?
Hello Colleen,
I found a doctor that would do surgery but, he explained it is painful or could potentially be dangerous. So I opted out of surgery. I live in Henderson, Nevada and he is a specialist. Either, I do surgery or live with this dreaded problem everyday. I think TMJ is also involved with this. I went to an allergist thinking it was my sinuses and he said I had an infection in my teeth. I am a dental assistant so, I knew it wasn’t that. Ibuprofen does help but, cant rely on that everyday. Take care Colleen!! Keep me in the loop!! Cindy
Hi- I was just told that my styloids are 3.8 mm and calcified, and that Eagle Syndrome is a possible diagnosis with more testing needed. I have cervical instability severe at C1-2, and herniation and nerve disruption C4-7. Is the Eagle Syndrome surgery only done in emergency situations and what constitutes an emergency? I am having so many symptoms and so much pain; it is unbearable. Thank you
I have just found out today I have eagle syndrome as well. TMJ dr, dentists, and finally after 5 years have my answers for all the pain and discomfort. I am a bit scared and worried that I would have to live with this till I can afford surgery without insurance.